AZX Wellness Hand Sanitizer

Manufacturer
ASC Marketing LTD
Effective date
2023-12-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:03:09

Label at a glance#

ProductAZX Wellness Hand Sanitizer
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

For hand washing to decrease bacteria on the skin.

Dosage and administration

Wet hands thoroughly for at least 20 seconds with product and allow to dry without wiping. Supervise children in the use of this product.

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80%

Purpose:

OTC - PURPOSE SECTION

Antiseptic

USES

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

WARNINGS

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flames. 

Do not use

OTC - DO NOT USE SECTION

in the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor 

OTC - STOP USE SECTION

if irritation or redness develop and persist for more than 72 hours. 

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact Poison Control Center right away. Store between 59-86°F (15-30°C). Avoid freezing and excessive heat above 104°F (40°C).

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly for at least 20 seconds with product and allow to dry without wiping. Supervise children in the use of this product.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

GLYCERIN, HYDROGEN PEROXIDE, METHYLCELLULOSE, STERILE WATER.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 gal1 gal

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041498ethanol 80 % Topical GelPSN2
1041498ethanol 0.8 ML/ML Topical GelSCD2
1041498ethanol 80 % Topical GelSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73145-007-01AZX Wellness Hand Sanitizer3780 mL in 1 BOTTLE, PUMPGEL37802

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73145-007AZX WELLNESS HAND SANITIZER (ALCOHOL) GEL [ASC MARKETING LTD]2Current NDC, Legacy NDC, 1 package rows20231202_b57c7e3a-f0bf-fd42-e053-2a95a90a3b4f.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73145-00773145-007-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AZX Wellness Hand SanitizerALCOHOLASC Marketing LTDb57c7e3a-f0bf-fd42-e053-2a95a90a3b4f2023-12-01WarningsExact identifier
ndc (package): 73145-007-01
ndc (product): 73145-007
ndc11 (package): 73145000701
spl id: 0b6dc42e-c0ac-b6cf-e063-6294a90aef5b
spl set id: b57c7e3a-f0bf-fd42-e053-2a95a90a3b4f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.